Other

Consistent with the company's policy of public data disclosure, this clinical trial results section includes result summaries of completed Lilly-sponsored clinical studies conducted on Lilly marketed products since July 1, 2004. The results of all Phase I, II, and III trials conducted in support of a product’s initial registration will be disclosed regardless of outcome, no later than when the first indication is approved and the drug is commercially available for patient use anywhere in the world. The results of all subsequent Phase II, III, and IV trials conducted after initial approval will be similarly disclosed within one year of trial completion. A trial’s results, irrespective of study phase, will be disclosed as soon as possible if there are significant safety findings.

Consistent with ICH E3 guidelines, Lilly will disclose the results of primary and secondary outcome measures that are specified in the study protocol, as well as additional safety and efficacy results that impact patient care and the use of our products. Also, Lilly discloses a comprehensive description of the trial design and methodology for each study. Results will be disclosed regardless of whether they support the hypothesis being tested or are contrary to the predicted outcome. Clinical trial results will be publicly disclosed as stated above, unless posting would compromise publication in a peer reviewed medical journal or contravene national laws or regulations. Results of studies that are under review by peer-reviewed journals that prohibit pre-publication disclosure will be posted on the registry at the time of publication. Clinical trial results are also disclosed through presentations and abstract submissions at professional scientific meetings.

The registry is also populated with the results of core efficacy and safety registration trials for products first approved after July 1, 1994.

Included are trial result summaries that are completed to date. The company will continue to disclose additional summaries and publication citations as they become available.

Summaries of clinical study results are intended to report the results of the study that were known at the time of each study's completion. The information contained in these summaries is not intended to promote or otherwise commercialize (directly or indirectly) any off-label or unapproved uses of Lilly medicines, nor is it intended to provide a comprehensive analysis of all data currently available regarding a particular drug. In some cases, more current information regarding a drug, including post-hoc analyses and meta-analyses, may be available as part of the general body of scientific knowledge in forms such as manuscripts, abstracts, or posters.

Clinical studies on Lilly products may also be sponsored and reported by parties other than Lilly in other clinical trial registries.

Trial Results

The following trials have been conducted for products in other therapeutic areas.

Drug Disease Trial ID Trial Title Trial
Phase
Cialis for Benign Prostatic Hyperplasia
Cialis
Benign Prostatic Hyperplasia
9120
A Multicenter, Parallel-Arm, Placebo-Controlled, Double-Blind Study to Evaluate the Efficacy and Safety of Tadalafil Administered Once Daily to Men with Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia
2
Cialis for Hypertension
Cialis
Hypertension
10077
A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy and Safety of Tadalafil (5 mg and 20 mg) Administered Once Daily to Subjects with Mild to Moderate Hypertension
2
Cymbalta for Fibromyalgia
Cymbalta
Fibromyalgia
6158
Duloxetine versus Placebo in the Treatment of Fibromyalgia Patients with or without Major Depressive Disorder
3
Cymbalta
Fibromyalgia
6222
Dose Response Study of Duloxetine Versus Placebo in the Treatment of Fibromyalgia Syndrome
3
Cymbalta
Fibromyalgia
9072
Duloxetine 60/120mg versus Placebo in the Treatment of Fibromyalgia
3
Cymbalta
Fibromyalgia
9075
A 1-Year Safety Study of Duloxetine in Patients with Fibromyalgia
3
Xigris for Severe Sepsis
Xigris
Severe Sepsis
1678
A Phase 3 Study to Determine the Efficacy and Safety for Recombinant Human Activated Protein C in Severe Sepsis
3
Xigris
Severe Sepsis
6716
Investigation of the Efficacy and Safety of Drotrecogin Alfa (Activated) in Pediatric Severe Sepsis
3
Xigris
Severe Sepsis
5771
Long-Term Follow-Up of Survivors from the PROWESS Trial (An Observational Study)
3b
Xigris
Severe Sepsis
6001
A Phase IIIb Study to Determine Efficacy and Safety of Extended Drotrecogin Alfa (Activated) Therapy in Patients with Persistent Requirement for Vasopressor Support After 96-Hour Infusion with Commercial Drotrecogin Alfa (Activated)
3b
Xigris
Severe Sepsis
6416
A Safety Evaluation Of Xigris [Drotrecogin Alfa (Activated)] In Hematoapoietic Stem Cell Transplant Patients With Severe Sepsis
3b
Xigris
Severe Sepsis
6669
Efficacy and Safety of Drotrecogin Alfa (activated) in Adult Patients with Early Stage Severe Sepsis
3b
Xigris
Severe Sepsis
7252
Efficacy and Safety of Drotrecogin Alfa (activated) in Adult Patients with Early Stage Severe Sepsis
3b
Xigris
Severe Sepsis
5502
An Open Label Study Of Drotrecogin Alfa (Activated) (LY203638) in Severe Sepsis
3 / 4
Xigris
Severe Sepsis
7159
An Open Label Study Of Drotrecogin Alfa (Activated) In Adult Patients With Severe Sepsis And Multiple Organ Dysfunctions: A Phase IV Protocol
4
Xigris
Severe Sepsis
6009
The Pharmacokinetics of Xigris® [Drotrecogin Alfa (Activated)] in Patients =160 kg with Severe Sepsis
4
Xigris
Severe Sepsis
6743
A Randomized, Double-Blind, Placebo-Controlled Trial of Prophylactic Heparin in Patients with Severe Sepsis and Higher Disease Severity Who Are Undergoing Treatment with Drotrecogin Alfa (Activated)
4
Yentreve: Clinical Pharmacology Study
Yentreve
Clinical Pharmacology Study
6867
A Placebo-Controlled Study of Electrophysiological Effects of Supratherapeutic Doses of Duloxetine on the QT Interval
1
Yentreve for Stress Urinary Incontinence
Yentreve
Stress Urinary Incontinence
1129
Duloxetine for Urinary Incontinence: A Multiple-Dose Study for Efficacy and Safety
2
Yentreve
Stress Urinary Incontinence
1604
Duloxetine Versus Placebo in the Relief of Stress Incontinence
2
Yentreve
Stress Urinary Incontinence
2595a
Biomechanical Effects of Duloxetine on Bladder Function and Sphincter Resistance During the Emptying Phase and on Urethral Cycle Function in Women with Pure Genuine Stress Incontinence
2
Yentreve
Stress Urinary Incontinence
2595b
Biomechanical Effects of Duloxetine on Bladder Function and Sphincter Resistance During the Emptying Phase and on Urethral Function During the Filling Phase of the Micturition Cycle in Women with Pure Genuine Stress Incontinence
2
Yentreve
Stress Urinary Incontinence
2615a
Efficacy and Safety of Duloxetine compared with Placebo, Pelvic Floor Muscle Training, and Combined Duloxetine/Pelvic Floor Muscle Training in Subjects with Moderate to Severe Stress Urinary Incontinence
2
Yentreve
Stress Urinary Incontinence
2615b
Efficacy and Safety of Duloxetine compared with Placebo, Pelvic Floor Muscle Training, and Combined Duloxetine/Pelvic Floor Muscle Training in Subjects with Moderate to Severe Stress Urinary Incontinence
2
Yentreve
Stress Urinary Incontinence
2624a
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects Electing Surgery for Severe Pure Genuine Stress Incontinence
2
Yentreve
Stress Urinary Incontinence
2624b
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects Electing Surgery for Severe Pure Genuine Stress Incontinence
2
Yentreve
Stress Urinary Incontinence
5308
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Symptoms of Bladder Overactivity Due to Pure Detrusor Instability or Sensory Urgency
2
Yentreve
Stress Urinary Incontinence
6984
Long-Term Monitoring of Safety in Subjects Treated with Duloxetine for Bladder Overactivity
2
Yentreve
Stress Urinary Incontinence
2685
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Stress Urinary Incontinence
3
Yentreve
Stress Urinary Incontinence
2686
Long-Term Monitoring of Safety in Subjects Treated with Duloxetine for Stress Urinary Incontinence
3
Yentreve
Stress Urinary Incontinence
2687
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Stress Urinary Incontinence
3
Yentreve
Stress Urinary Incontinence
2688
Long-Term Monitoring of Safety in Subjects Treated with Duloxetine for Stress Urinary Incontinence
3
Yentreve
Stress Urinary Incontinence
2689
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Stress Urinary Incontinence
3
Yentreve
Stress Urinary Incontinence
2690
Long-Term Monitoring of Safety in Subjects Treated with Duloxetine for Stress Urinary Incontinence
3
Yentreve
Stress Urinary Incontinence
3171
Prospective Outcomes of Duloxetine in Usual Naturalistic Care in Women with Stress Urinary Incontinence
3
Yentreve
Stress Urinary Incontinence
5309
Long-Term Monitoring of Safety in Subjects Treated with Duloxetine for Stress Urinary Incontinence
3
Yentreve
Stress Urinary Incontinence
6231
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Stress Urinary Incontinence
3
Yentreve
Stress Urinary Incontinence
6232
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Stress Urinary Incontinence
3
Yentreve
Stress Urinary Incontinence
6192a
Efficacy and Safety of Duloxetine Compared with Placebo in Women with Symptoms of Mixed Urinary Incontinence
3B
Yentreve
Stress Urinary Incontinence
6192b
Efficacy and Safety of Duloxetine Compared with Placebo in Women with Symptoms of Mixed Urinary Incontinence
3B
Yentreve
Stress Urinary Incontinence
6195a
The Effectiveness of Duloxetine Compared with Placebo in the Treatment of Predominant Stress Urinary Incontinence
3B
Yentreve
Stress Urinary Incontinence
6195b
The Effectiveness of Duloxetine Compared with Placebo in the Treatment of Predominant Stress Urinary Incontinence
3B
Yentreve
Stress Urinary Incontinence
8049
The Safety and Effectiveness of Duloxetine Compared with Placebo and its Long-term Safety and Efficacy in the Treatment of Predominant Stress Urinary Incontinence.
3B
Yentreve
Stress Urinary Incontinence
9587
Effect of Duloxetine on Valsalva Leak Point Pressure and Quantitative Rhabdosphincter Electromyography Measures in Women with Stress Urinary Incontinence
3B
Yentreve
Stress Urinary Incontinence
8363
Study of Duloxetine HCl in Women of Different Demographic Characteristics and Comorbidities with Stress Urinary Incontinence: Evaluation of Efficacy and Safety
4
Yentreve
Stress Urinary Incontinence
8672
Duloxetine versus Placebo in the Treatment of Community-Dwelling Women Aged 65 Years or Older with Stress or Stress-Predominant Mixed Urinary Incontinence
4